Structure Content

Département: Institut de l’Audition – Centre de l’Institut Pasteur

Tous Publications

2024
Mendia C, Peineau T, Zamani M, Felgerolle C, Yahiaoui N, Christophersen N, Papal S, Maudoux A, Maroofian R, Patni P, Nouaille S, Bowl MR, Delmaghani S, Galehdari H, Vona B, Dulon D, Vitry S, El-Amraoui A, Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss., Mol Ther 2024 Jan; (): .
2024
Ghizlene Lahlou, Charlotte Calvet, François Simon, Vincent Michel, Lauranne Alciato, Baptiste Plion, Jacques Boutet de Monvel, Marie-José Lecomte, Mathieu Beraneck, Christine Petit, Saaid Safieddine, Extended timeframe for restoring inner ear function through gene therapy in Usher1G preclinical model, JCI Insight, In press, ⟨10.1172/jci.insight.169504⟩.
2023
Boëda B, Michel V, Etournay R, England P, Rigaud S, Mary H, Gobaa S, Etienne-Manneville S, SCRIB controls apical contractility during epithelial differentiation., J Cell Biol 2023 Dec; 222(12): .
2023
Brunstein M, Lubetzki J, Moutoussamy C, Li W, Barral J, Fast 2-photon stimulation using holographic patterns., Opt Express 2023 Nov; 31(23): 39222-39238.
2023
Wang X, Delgado J, Marchesotti S, Kojovic N, Sperdin HF, Rihs TA, Schaer M, Giraud AL, Speech reception in young children with autism is selectively indexed by a neural oscillation coupling anomaly., J Neurosci 2023 Aug; (): .
2023
Jean P, Wong Jun Tai F, Singh-Estivalet A, Lelli A, Scandola C, Megharba S, Schmutz S, Roux S, Mechaussier S, Sudres M, Mouly E, Heritier AV, Bonnet C, Mallet A, Novault S, Libri V, Petit C, Michalski N, Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies., Proc Natl Acad Sci U S A 2023 Jun; 120(26): e2221744120.
2023
Amariutei AE, Jeng JY, Safieddine S, Marcotti W, Recent advances and future challenges in gene therapy for hearing loss., R Soc Open Sci 2023 Jun; 10(6): 230644.
2023
Mazuecos L, Alberdi P, Hernández-Jarguín A, Contreras M, Villar M, Cabezas-Cruz A, Simo L, González-García A, Díaz-Sánchez S, Neelakanta G, Bonnet SI, Fikrig E, de la Fuente J, Frankenbacteriosis targeting interactions between pathogen and symbiont to control infection in the tick vector., iScience 2023 May; 26(5): 106697.
2023
Christine Petit, Crystel Bonnet, Saaïd Safieddine, Deafness: from genetic architecture to gene therapy, Nature Reviews Genetics, 2023, ⟨10.1038/s41576-023-00597-7⟩.
2023
Gourévitch B, Pitts T, Iceman K, Reed M, Cai J, Chu T, Zeng W, Morgado-Valle C, Mellen N, Synchronization of inspiratory burst onset along the ventral respiratory column in the neonate mouse is mediated by electrotonic coupling., BMC Biol 2023 Apr; 21(1): 83.
2023
Lahlou G, Calvet C, Giorgi M, Lecomte MJ, Safieddine S, Towards the Clinical Application of Gene Therapy for Genetic Inner Ear Diseases., J Clin Med 2023 Jan; 12(3): .
2023
Brazier F, Courbebaisse M, David A, Bergerat D, Leroy C, Lindner M, Maruani G, Saint Jacques C, Letavernier E, Hureaux M, Vargas-Poussou R, Prié D, Relationship between clinical phenotype and in vitro analysis of 13 NPT2c/SCL34A3 mutants., Sci Rep 2023 Jan; 13(1): 85.
2023
Souffi S, Varnet L, Zaidi M, Bathellier B, Huetz C, Edeline JM, , Reduction in sound discrimination in noise is related to envelope similarity and not to a decrease in envelope tracking abilities., J Physiol 2023 Jan; 601(1): 123-149.
2022
Calvet C, Peineau T, Benamer N, Cornille M, Lelli A, Plion B, Lahlou G, Fanchette J, Nouaille S, Boutet de Monvel J, Estivalet A, Jean P, Michel V, Sachse M, Michalski N, Avan P, Petit C, Dulon D, Safieddine S, The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses., iScience 2022 Dec; 25(12): 105628.
2022
Verdier A, Dominique N, Groussard D, Aldanondo A, Bathellier B, Bagur S, , Enhanced perceptual task performance without deprivation in mice using medial forebrain bundle stimulation., Cell Rep Methods 2022 Dec; 2(12): 100355.
2022
Audouard E, Michel F, Pierroz V, Kim T, Rousselot L, Gillet-Legrand B, Dufayet-Chauffaut G, Buchmann P, Florea M, Khel A, Altynbekova K, Delgaldo C, Escudero E, Soler ABA, Cartier N, Piguet F, Folcher M, , Bioelectronic cell-based device provides a strategy for the treatment of the experimental model of multiple sclerosis., J Control Release 2022 Nov; 352(): 994-1008.
2022
Filipchuk A, Schwenkgrub J, Destexhe A, Bathellier B, , Awake perception is associated with dedicated neuronal assemblies in the cerebral cortex., Nat Neurosci 2022 Oct; 25(10): 1327-1338.
2022
Trébeau C, de Monvel JB, Altay G, Tinevez JY, Etournay R, , Extracting multiple surfaces from 3D microscopy images in complex biological tissues with the Zellige software tool., BMC Biol 2022 08; 20(1): 183.
2022
Aigrot MS, Barthelemy C, Moyon S, Dufayet-Chaffaud G, Izagirre-Urizar L, Gillet-Legrand B, Tada S, Bayón-Cordero L, Chara JC, Matute C, Cartier N, Lubetzki C, Tepavčević V, , Genetically modified macrophages accelerate myelin repair., EMBO Mol Med 2022 Aug; 14(8): e14759.
2022
Aziz El-Amraoui, Gwenaelle G S Géléoc, Usher syndrome Recent advances in our understanding of genes and therapeutics, Research Outreach, 2022, 131, ⟨10.32907/RO-131-3039996892⟩.
2022
Renard A, Harrell ER, Bathellier B, , Olfactory modulation of barrel cortex activity during active whisking and passive whisker stimulation., Nat Commun 2022 Jul; 13(1): 3830.
2022
Sedigheh Delmaghani, Aziz El-Amraoui, Déficience auditive induite par le bruit : comment peut-elle être prévenue et traitée ?, Planet-Vie, 2022.
2022
Ceballo S, Deneux T, Siliceo M, Bathellier B, , Differential roles of auditory and visual cortex for sensory detection in mice., C R Biol 2022 May; 345(1): 75-89.
2022
Marin N, Lobo Cerna F, Barral J, Signatures of cochlear processing in neuronal coding of auditory information., Mol Cell Neurosci 2022 May; 120(): 103732.
2022
Audrey Maudoux, Sandrine Vitry, Aziz El-Amraoui, Vestibular Deficits in Deafness: Clinical Presentation, Animal Modeling, and Treatment Solutions, Frontiers in Neurology, 2022, 13, pp.816534. ⟨10.3389/fneur.2022.816534⟩.
2022
Sedigheh Delmaghani, Aziz El-Amraoui, The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification, Human Genetics, 2022, 141 (3-4), pp.709-735. ⟨10.1007/s00439-022-02448-7⟩.
2022
Sailor KA, Agoranos G, López-Manzaneda S, Tada S, Gillet-Legrand B, Guerinot C, Masson JB, Vestergaard CL, Bonner M, Gagnidze K, Veres G, Lledo PM, Cartier N, , Hematopoietic stem cell transplantation chemotherapy causes microglia senescence and peripheral macrophage engraftment in the brain., Nat Med 2022 Mar; 28(3): 517-527.
2022
Wysocka EM, Page M, Snowden J, Simpson TI, , Comparison of rule- and ordinary differential equation-based dynamic model of DARPP-32 signalling network., PeerJ 2022 ; 10(): e14516.
2021
Harrell ER, Renard A, Bathellier B, , Fast cortical dynamics encode tactile grating orientation during active touch., Sci Adv 2021 Sep; 7(36): eabf7096.
2021
Aziz El-Amraoui, Vieillissement de l’oreille interne : bases génétiques et conséquences à l’échelle cellulaire et moléculaire., Le vieillissement cochléo-vestibulaire : Rapport SFORL 2021, Elsevier Masson, pp.23-34, 2021, 9782294772948.
2021
Khamsing D, Lebrun S, Fanget I, Larochette N, Tourain C, de Sars V, Brunstein M, Oheim M, Carrel D, Darchen F, Desnos C, , A role for BDNF- and NMDAR-induced lysosomal recruitment of mTORC1 in the regulation of neuronal mTORC1 activity., Mol Brain 2021 07; 14(1): 112.
2021
Barbara Vona, Neda Mazaheri, Sheng-Jia Lin, Lucy A Dunbar, Reza Maroofian, Hela Azaiez, Kevin T Booth, Sandrine Vitry, Aboulfazl Rad, Franz Rüschendorf, Pratishtha Varshney, Ben Fowler, Christian Beetz, Kumar N Alagramam, David Murphy, Gholamreza Shariati, Alireza Sedaghat, Henry Houlden, Cassidy Petree, Shruthi Vijaykumar, Richard J H Smith, Thomas Haaf, Aziz El-Amraoui, Michael R Bowl, Gaurav K Varshney, Hamid Galehdari, A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans, Human Genetics, 2021, 140 (6), pp.915 - 931. ⟨10.1007/s00439-020-02254-z⟩.
2021
Eric Nisenbaum, Torin Thielhelm, Aida Nourbakhsh, Denise Yan, Susan Blanton, Yilai Shu, Karl Koehler, Aziz El-Amraoui, Zhengyi Chen, Byron Lam, Xuezhong Liu, Review of Genotype-Phenotype Correlations in Usher Syndrome, Ear & Hearing, 2022, 43 (1), pp.1-8. ⟨10.1097/AUD.0000000000001066⟩.
2021
Sorokina O, Mclean C, Croning MDR, Heil KF, Wysocka E, He X, Sterratt D, Grant SGN, Simpson TI, Armstrong JD, , A unified resource and configurable model of the synapse proteome and its role in disease., Sci Rep 2021 May; 11(1): 9967.
2021
Aida Nourbakhsh, Brett M. Colbert, Eric Nisenbaum, Aziz El-Amraoui, Derek M. Dykxhoorn, Karl Russell Koehler, Zheng-Yi Chen, Xue Z. Liu, Stem Cells and Gene Therapy in Progressive Hearing Loss: the State of the Art, Journal of the Association for Research in Otolaryngology, 2021, 22 (2), pp.95-105. ⟨10.1007/s10162-020-00781-0⟩.
2021
Bondanelli G, Deneux T, Bathellier B, Ostojic S, , Network dynamics underlying OFF responses in the auditory cortex., Elife 2021 03; 10(): .
2021
Audouard E, Oger V, Meha B, Cartier N, Sevin C, Piguet F, , Complete Correction of Brain and Spinal Cord Pathology in Metachromatic Leukodystrophy Mice., Front Mol Neurosci 2021 ; 14(): 677895.
2021
Catherine Botto, Deniz Dalkara, Aziz El-Amraoui, Progress in Gene Editing Tools and Their Potential for Correcting Mutations Underlying Hearing and Vision Loss, Frontiers in Genome Editing, 2021, 3, pp.737632. ⟨10.3389/fgeed.2021.737632⟩.
2020
Boucher S, Tai FWJ, Delmaghani S, Lelli A, Singh-Estivalet A, Dupont T, Niasme-Grare M, Michel V, Wolff N, Bahloul A, Bouyacoub Y, Bouccara D, Fraysse B, Deguine O, Collet L, Thai-Van H, Ionescu E, Kemeny JL, Giraudet F, Lavieille JP, Devèze A, Roudevitch-Pujol AL, Vincent C, Renard C, Franco-Vidal V, Thibult-Apt C, Darrouzet V, Bizaguet E, Coez A, Aschard H, Michalski N, Lefevre GM, Aubois A, Avan P, Bonnet C, Petit C, , Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis., Proc Natl Acad Sci U S A 2020 12; 117(49): 31278-31289.
2020
Schwenkgrub J, Harrell ER, Bathellier B, Bouvier J, , Deep imaging in the brainstem reveals functional heterogeneity in V2a neurons controlling locomotion., Sci Adv 2020 Dec; 6(49): .
2020
Zhu Y, Delhommel F, Cordier F, Lüchow S, Mechaly A, Colcombet-Cazenave B, Girault V, Pepermans E, Bahloul A, Gautier C, Brûlé S, Raynal B, Hoos S, Haouz A, Caillet-Saguy C, Ivarsson Y, Wolff N, , Deciphering the Unexpected Binding Capacity of the Third PDZ Domain of Whirlin to Various Cochlear Hair Cell Partners., J Mol Biol 2020 11; 432(22): 5920-5937.
2020
Gwenaelle G S Géléoc, Aziz El-Amraoui, Disease mechanisms and gene therapy for Usher syndrome, Hearing Research, 2020, 394, pp.107932. ⟨10.1016/j.heares.2020.107932⟩.
2020
Harrell ER, Goldin MA, Bathellier B, Shulz DE, , An elaborate sweep-stick code in rat barrel cortex., Sci Adv 2020 Sep; 6(38): .
2020
Lindner M, Mehel H, David A, Leroy C, Burtin M, Friedlander G, Terzi F, Mika D, Fischmeister R, Prié D, Fibroblast growth factor 23 decreases PDE4 expression in heart increasing the risk of cardiac arrhythmia; Klotho opposes these effects., Basic Res Cardiol 2020 Jul; 115(5): 51.
2020
Sedigheh Delmaghani, Aziz El-Amraoui, Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges, Journal of Clinical Medicine, 2020, 9 (7), pp.2309. ⟨10.3390/jcm9072309⟩.
2020
Karam S, Margaria JP, Bourcier A, Mika D, Varin A, Bedioune I, Lindner M, Bouadjel K, Dessillons M, Gaudin F, Lefebvre F, Mateo P, Lechène P, Gomez S, Domergue V, Robert P, Coquard C, Algalarrondo V, Samuel JL, Michel JB, Charpentier F, Ghigo A, Hirsch E, Fischmeister R, Leroy J, Vandecasteele G, Cardiac Overexpression of PDE4B Blunts β-Adrenergic Response and Maladaptive Remodeling in Heart Failure., Circulation 2020 Jul; 142(2): 161-174.
2020
Oheim M, Salomon A, Brunstein M, , Supercritical Angle Fluorescence Microscopy and Spectroscopy., Biophys J 2020 05; 118(10): 2339-2348.
2020
Cherine Charfeddine, Hamza Dallali, Ghaith Abdessalem, Kais Ghedira, Yosr Hamdi, Sahar Elouej, Zied Landoulsi, Valérie Delague, Arnaud Lagarde, Nicolas Levy, Aziz El-Amraoui, Mohamed Samir Boubaker, Sonia Abdelhak, Mourad Mokni, Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family, Journal of Human Genetics, 2020, 65 (4), pp.397 - 410. ⟨10.1038/s10038-019-0711-4⟩.
2020
Kaitlin Szederkenyi, Bruno Lagarde, Maia Brunstein, Marc Guillon, Christopher M.Yip and Martin Oheim, Investigating Polarisation Effects in a Confocal Total Internal Reflection-Supercritical Angle Fluorescence (TIR-SAF) Geometry with Sample Scanning, Vol. 118.
2019
Hardelin JP, Safieddine S, [Congenital deafness forms: progressing toward gene therapy?]., Med Sci (Paris) 2019 Dec; 35(12): 1213-1215.
2019
Johnson SL, Safieddine S, Mustapha M, Marcotti W, Hair Cell Afferent Synapses: Function and Dysfunction., Cold Spring Harb Perspect Med 2019 Dec; 9(12): .
2019
Oheim M, Salomon A, Weissman A, Brunstein M, Becherer U, , Calibrating Evanescent-Wave Penetration Depths for Biological TIRF Microscopy., Biophys J 2019 09; 117(5): 795-809.
2019
Barral J, Wang XJ, Reyes AD, Propagation of temporal and rate signals in cultured multilayer networks., Nat Commun 2019 Sep; 10(1): 3969.
2019
Lucy A Dunbar, Pranav Patni, Carlos Aguilar, Philomena Mburu, Laura Corns, Helena Rr Wells, Sedigheh Delmaghani, Andrew Parker, Stuart Johnson, Debbie Williams, Christopher T Esapa, Michelle M Simon, Lauren Chessum, Sherylanne Newton, Joanne Dorning, Prashanthini Jeyarajan, Susan Morse, Andrea Lelli, Gemma F Codner, Thibault Peineau, Suhasini R Gopal, Kumar N Alagramam, Ronna Hertzano, Didier Dulon, Sara Wells, Frances M Williams, Christine Petit, Sally J Dawson, Steve Dm Brown, Walter Marcotti, Aziz El-Amraoui, Michael R Bowl, Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function, EMBO Molecular Medicine, 2019, 11 (9), pp.e10288. ⟨10.15252/emmm.201910288⟩.
2019
Mika D, Bobin P, Lindner M, Boet A, Hodzic A, Lefebvre F, Lechène P, Sadoune M, Samuel JL, Algalarrondo V, Rucker-Martin C, Lambert V, Fischmeister R, Vandecasteele G, Leroy J, Synergic PDE3 and PDE4 control intracellular cAMP and cardiac excitation-contraction coupling in a porcine model., J Mol Cell Cardiol 2019 Aug; 133(): 57-66.
2019
Liu D, Wang Z, Nicolas V, Lindner M, Mika D, Vandecasteele G, Fischmeister R, Brenner C, PDE2 regulates membrane potential, respiration and permeability transition of rodent subsarcolemmal cardiac mitochondria., Mitochondrion 2019 Jul; 47(): 64-75.
2019
Schilder AGM, Su MP, Blackshaw H, Lustig L, Staecker H, Lenarz T, Safieddine S, Gomes-Santos CS, Holme R, Warnecke A, Hearing Protection, Restoration, and Regeneration: An Overview of Emerging Therapeutics for Inner Ear and Central Hearing Disorders., Otol Neurotol 2019 Jun; 40(5): 559-570.
2019
Deneux T, Harrell ER, Kempf A, Ceballo S, Filipchuk A, Bathellier B, , Context-dependent signaling of coincident auditory and visual events in primary visual cortex., Elife 2019 05; 8(): .
2019
Tertrais M, Bouleau Y, Emptoz A, Belleudy S, Sutton RB, Petit C, Safieddine S, Dulon D, Viral Transfer of Mini-Otoferlins Partially Restores the Fast Component of Exocytosis and Uncovers Ultrafast Endocytosis in Auditory Hair Cells of Otoferlin Knock-Out Mice., J Neurosci 2019 May; 39(18): 3394-3411.
2019
Defourny J, Aghaie A, Perfettini I, Avan P, Delmaghani S, Petit C, , Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage., Proc. Natl. Acad. Sci. U.S.A. 2019 04; 116(16): 8010-8017.
2019
Ceballo S, Bourg J, Kempf A, Piwkowska Z, Daret A, Pinson P, Deneux T, Rumpel S, Bathellier B, , Cortical recruitment determines learning dynamics and strategy., Nat Commun 2019 Apr; 10(1): 1479.
2019
Akil O, Dyka F, Calvet C, Emptoz A, Lahlou G, Nouaille S, Boutet de Monvel J, Hardelin JP, Hauswirth WW, Avan P, Petit C, Safieddine S, Lustig LR, Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model., Proc Natl Acad Sci U S A 2019 Mar; 116(10): 4496-4501.
2019
Rakotoson I, Delhomme B, Djian P, Deeg A, Brunstein M, Seebacher C, Uhl R, Ricard C, Oheim M, , Fast 3-D Imaging of Brain Organoids With a New Single-Objective Planar-Illumination Two-Photon Microscope., Front Neuroanat 2019 ; 13(): 77.
2018
Brunstein M, Salomon A, Oheim M, , Decoding the Information Contained in Fluorophore Radiation Patterns., ACS Nano 2018 12; 12(12): 11725-11730.
2018
Trébeau C, Boutet de Monvel J, Wong Jun Tai F, Petit C, Etournay R, DNABarcodeCompatibility: an R-package for optimizing DNA-barcode combinations in multiplex sequencing experiments, Bioinformatics 2018 Dec;.
2018
Aubin Samacoits, Racha Chouaib, Adham Safieddine, Abdel-Meneem Traboulsi, Christophe Zimmer, Wei Ouyang, Marion Peter, Edouard Bertrand, Thomas Walter, Florian Mueller, A computational framework to study sub-cellular RNA localization, Nature Communications, 2018, 9 (1), pp.4584. ⟨10.1038/s41467-018-06868-w⟩.
2018
Dussaux C, Szabo V, Chastagnier Y, Fodor J, Léger JF, Bourdieu L, Perroy J, Ventalon C, , Fast confocal fluorescence imaging in freely behaving mice., Sci Rep 2018 Nov; 8(1): 16262.
2018
M. Oheim and M. Brunstein, Quantifying Colocalisation in Biological Fluorescence Micrsocopy, eLS.
2018
Kuchibhotla K, Bathellier B, , Neural encoding of sensory and behavioral complexity in the auditory cortex., Curr Opin Neurobiol 2018 Oct; 52(): 65-71.
2018
Calvet C, Lahlou G, Safieddine S, [Gene therapy progress: hopes for Usher syndrome]., Med Sci (Paris) 2018 Oct; 34(10): 842-848.
2018
Corns LF, Johnson SL, Roberts T, Ranatunga KM, Hendry A, Ceriani F, Safieddine S, Steel KP, Forge A, Petit C, Furness DN, Kros CJ, Marcotti W, Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation., Nat Commun 2018 Oct; 9(1): 4015.
2018
Dulon D, Papal S, Patni P, Cortese M, Vincent PF, Tertrais M, Emptoz A, Tlili A, Bouleau Y, Michel V, Delmaghani S, Aghaie A, Pepermans E, Alegria-Prevot O, Akil O, Lustig L, Avan P, Safieddine S, Petit C, El-Amraoui A, Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome., J Clin Invest 2018 Aug; 128(8): 3382-3401.
2018
Puy V, Darwiche W, Trudel S, Gomila C, Lony C, Puy L, Lefebvre T, Vitry S, Boullier A, Karim Z, Ausseil J, , Predominant role of microglia in brain iron retention in Sanfilippo syndrome, a pediatric neurodegenerative disease., Glia 2018 08; 66(8): 1709-1723.
2018
K.T. Booth, K. Kahrizi, M. Babanejad, H. Daghagh, G. Bademci, S. Arzhangi, D. Zareabdollahi, D. Duman, A. El-Amraoui, M. Tekin, H. Najmabadi, H. Azaiez, R.J. Smith, Variants in CIB2 cause DFNB48 and not USH1J, Clinical Genetics, 2018, 93 (4), pp.812-821. ⟨10.1111/cge.13170⟩.
2018
Bhukhai K, de Dreuzy E, Giorgi M, Colomb C, Negre O, Denaro M, Gillet-Legrand B, Cheuzeville J, Paulard A, Trebeden-Negre H, Borwornpinyo S, Sii-Felice K, Maouche L, Down JD, Leboulch P, Payen E, , Ex Vivo Selection of Transduced Hematopoietic Stem Cells for Gene Therapy of β-Hemoglobinopathies., Mol Ther 2018 Feb; 26(2): 480-495.
2018
Alix Trouillet, Elisabeth Dubus, Julie Degardin, Amrit Estivalet, Ivana Ivkovic, David Godefroy, Diego García-Ayuso, Manuel Simonutti, Iman Sahly, José-Alain Sahel, Aziz El-Amraoui, Christine Petit, Serge Picaud, Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments, Scientific Reports, 2018, 8 (1), pp.1968. ⟨10.1038/s41598-018-20171-0⟩.
2018
Barral J, Jülicher F, Martin P, Friction from Transduction Channels’ Gating Affects Spontaneous Hair-Bundle Oscillations., Biophys J 2018 Jan; 114(2): 425-436.
2017
Vincent Michel, Kevin T Booth, Pranav Patni, Matteo Cortese, Hela Azaiez, Amel Bahloul, Kimia Kahrizi, Ménélik Labbe, Alice Emptoz, Andrea Lelli, Julie Dégardin, Typhaine Dupont, Asadollah Aghaie, Danuta Oficjalska‐pham, Serge Picaud, Hossein Najmabadi, Richard J Smith, Michael R Bowl, Steven Dm Brown, Paul Avan, Christine Petit, Aziz El‐amraoui, CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival, EMBO Molecular Medicine, 2017, 9 (12), pp.1711 - 1731. ⟨10.15252/emmm.201708087⟩.
2017
Michalski N, Goutman JD, Auclair SM, Boutet de Monvel J, Tertrais M, Emptoz A, Parrin A, Nouaille S, Guillon M, Sachse M, Ciric D, Bahloul A, Hardelin JP, Sutton RB, Avan P, Krishnakumar SS, Rothman JE, Dulon D, Safieddine S, Petit C, Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses., Elife 2017 Nov; 6(): .
2017
Dye NA, Popović M, Spannl S, Etournay R, Kainmüller D, Ghosh S, Myers EW, Jülicher F, Eaton S, Cell dynamics underlying oriented growth of the wing imaginal disc, Development 2017 12;144(23):4406-4421.
2017
Emptoz A, Michel V, Lelli A, Akil O, Boutet de Monvel J, Lahlou G, Meyer A, Dupont T, Nouaille S, Ey E, Franca de Barros F, Beraneck M, Dulon D, Hardelin JP, Lustig L, Avan P, Petit C, Safieddine S, Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G., Proc Natl Acad Sci U S A 2017 Sep; 114(36): 9695-9700.
2017
Amel Bahloul, Elise Pepermans, Bertrand Raynal, Nicolas Wolff, Florence Cordier, Patrick England, Sylvie Nouaille, Bruno Baron, Aziz El-Amraoui, Jean-Pierre Hardelin, Dominique Durand, Christine Petit, Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery, FEBS Letters, 2017, 591 (15), pp.2299 - 2310. ⟨10.1002/1873-3468.12729⟩.
2017
Bossou YM, Serssar Y, Allou A, Vitry S, Momas I, Seta N, Menotti J, Achard S, , Impact of Mycotoxins Secreted by Aspergillus Molds on the Inflammatory Response of Human Corneal Epithelial Cells., Toxins (Basel) 2017 06; 9(7): .
2017
Barral J, Reyes AD, Optogenetic Stimulation and Recording of Primary Cultured Neurons with Spatiotemporal Control., Bio Protoc 2017 Jun; 7(12): .
2017
Cataldo Schietroma, Karine Parain, Amrit Estivalet, Asadollah Aghaie, Jacques Boutet de Monvel, Serge Picaud, José-Alain Sahel, Muriel Perron, Aziz El-Amraoui, Christine Petit, Usher syndrome type 1–associated cadherins shape the photoreceptor outer segment, Journal of Cell Biology, 2017, 216 (6), pp.1849 - 1864. ⟨10.1083/jcb.201612030⟩.
2017
Roland B, Deneux T, Franks KM, Bathellier B, Fleischmann A, , Odor identity coding by distributed ensembles of neurons in the mouse olfactory cortex., Elife 2017 May; 6(): .
2017
Brunstein M, Roy L, Oheim M, , Near-Membrane Refractometry Using Supercritical Angle Fluorescence., Biophys J 2017 May; 112(9): 1940-1948.
2017
Philippe F.Y. Vincent, Yohan Bouleau, Gilles Charpentier, Alice Emptoz, Saaid Safieddine, Christine Petit, Didier Dulon, Different Ca V 1.3 Channel Isoforms Control Distinct Components of the Synaptic Vesicle Cycle in Auditory Inner Hair Cells, Journal of Neuroscience, 2017, 37 (11), pp.2960-2975. ⟨10.1523/JNEUROSCI.2374-16.2017⟩.
2017
Matteo Cortese, Samantha Papal, Francisco Pisciottano, Ana Belén Elgoyhen, Jean-Pierre Hardelin, Christine Petit, Lucia Florencia Franchini, Aziz El-Amraoui, Spectrin βV adaptive mutations and changes in subcellular location correlate with emergence of hair cell electromotility in mammalians., Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 (8), pp.2054-2059. ⟨10.1073/pnas.1618778114⟩.
2017
Brunstein M, Oheim M, , Dependence of descriptors of co-localization on microscope spatiotemporal resolution and the choice of regions of interest., Microsc Res Tech 2017 Feb; 80(2): 220-230.
2017
Vettel C, Lindner M, Dewenter M, Lorenz K, Schanbacher C, Riedel M, Lämmle S, Meinecke S, Mason FE, Sossalla S, Geerts A, Hoffmann M, Wunder F, Brunner FJ, Wieland T, Mehel H, Karam S, Lechêne P, Leroy J, Vandecasteele G, Wagner M, Fischmeister R, El-Armouche A, Phosphodiesterase 2 Protects Against Catecholamine-Induced Arrhythmia and Preserves Contractile Function After Myocardial Infarction., Circ Res 2017 Jan; 120(1): 120-132.
2017
Schwenkgrub J, Zaremba M, Joniec-Maciejak I, Cudna A, Mirowska-Guzel D, Kurkowska-Jastrzębska I, , The phosphodiesterase inhibitor, ibudilast, attenuates neuroinflammation in the MPTP model of Parkinson’s disease., PLoS One 2017 ; 12(7): e0182019.
2017
Brunner C, Isabel C, Martin A, Dussaux C, Savoye A, Emmrich J, Montaldo G, Mas JL, Baron JC, Urban A, , Mapping the dynamics of brain perfusion using functional ultrasound in a rat model of transient middle cerebral artery occlusion., J Cereb Blood Flow Metab 2017 Jan; 37(1): 263-276.
2016
Crystel Bonnet, Zied Riahi, Sandra Chantot-Bastaraud, Luce Smagghe, Mélanie Letexier, Charles Marcaillou, Gaëlle Lefèvre, Jean-Pierre Hardelin, Aziz El-Amraoui, Amrit Singh-Estivalet, Saddek Mohand-Saïd, Susanne Kohl, Anne Kurtenbach, Ieva Sliesoraityte, Ditta Zobor, Souad Gherbi, Francesco Testa, Francesca Simonelli, Sandro Banfi, Ana Fakin, Damjan Glavač, Martina Jarc-Vidmar, Andrej Zupan, Saba Battelino, Loreto Martorell Sampol, Maria Antonia Claveria, Jaume Catala Mora, Shzeena Dad, Lisbeth Møller, Jesus Rodriguez Jorge, Marko Hawlina, Alberto Auricchio, José-Alain Sahel, Sandrine Marlin, Eberhart Zrenner, Isabelle Audo, Christine Petit, An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients, European Journal of Human Genetics, 2016, 24 (12), pp.1730-1738. ⟨10.1038/ejhg.2016.99⟩.
2016
Barral J, D Reyes A, Synaptic scaling rule preserves excitatory-inhibitory balance and salient neuronal network dynamics., Nat Neurosci 2016 Dec; 19(12): 1690-1696.
2016
El-Amraoui A, Petit C, Cadherins in the auditory sensory organ, Shintaro T. Suzuki & Shinji Hirano (eds.), In The Cadherin Superfamily, Springer, Japan. pp 341-361 (2016).
2016
Paul K Potter, Michael R Bowl, Prashanthini Jeyarajan, Laura Wisby, Andrew Blease, Michelle E Goldsworthy, Michelle M Simon, Simon Greenaway, Vincent Michel, Alun Barnard, Carlos Aguilar, Thomas Agnew, Gareth Banks, Andrew Blake, Lauren Chessum, Joanne Dorning, Sara Falcone, Laurence Goosey, Shelley Harris, Andy Haynes, Ines Heise, Rosie Hillier, Tertius Hough, Angela Hoslin, Marie Hutchison, Ruairidh King, Saumya Kumar, Heena V Lad, Gemma Law, Robert E Maclaren, Susan Morse, Thomas Nicol, Andrew Parker, Karen Pickford, Siddharth Sethi, Becky Starbuck, Femke Stelma, Michael Cheeseman, Sally H Cross, Russell G Foster, Ian J Jackson, Stuart N Peirson, Rajesh V Thakker, Tonia Vincent, Cheryl Scudamore, Sara Wells, Aziz El-Amraoui, Christine Petit, Abraham Acevedo-Arozena, Patrick M Nolan, Roger Cox, Anne-Marie Mallon, Steve D M Brown, Novel gene function revealed by mouse mutagenesis screens for models of age-related disease, Nature Communications, 2016, 7, pp.12444. ⟨10.1038/ncomms12444⟩.
2016
Aziz El-Amraoui, Christine Petit, Cadherins in the Auditory Sensory Organ, Suzuki, S; Hirano, S. The Cadherin Superfamily, Springer, pp.341 - 361, 2016, 978-4-431-56033-3. ⟨10.1007/978-4-431-56033-3_13⟩.
2016
Zhang QJ, Han B, Lan L, Zong L, Shi W, Wang HY, Xie LY, Wang H, Zhao C, Zhang C, Yin ZF, Wang DY, Petit C, Guan J, Wang QJ, High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder, Clin. Genet. 2016 Jan;.
2016
Andrea Lelli, Vincent Michel, Jacques Boutet de Monvel, Matteo Cortese, Montserrat Bosch-Grau, Asadollah Aghaie, Isabelle Perfettini, Typhaine Dupont, Paul Avan, Aziz El-Amraoui, Christine Petit, Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth., Journal of Cell Biology, 2016, 212 (2), pp.231-44. ⟨10.1083/jcb.201509017⟩.
2016
Bedioune I, Bobin P, Karam S, Lindner M, Mika D, Lechêne P, Leroy J, Fischmeister R, Vandecasteele G, [Cyclic nucleotide phosphodiesterases: role in the heart and therapeutic perspectives]., Biol Aujourdhui 2016 ; 210(3): 127-138.
2015
Brunstein M, Cattoni A, Estrada L, Yacomotti AM, , Improving image contrast in fluorescence microscopy with nanostructured substrates., Opt Express 2015 Nov; 23(23): 29772-8.
2015
Vincent PF, Bouleau Y, Petit C, Dulon D, A synaptic F-actin network controls otoferlin-dependent exocytosis in auditory inner hair cells, Elife 2015;4.
2015
Delmaghani S, Defourny J, Aghaie A, Beurg M, Dulon D, Thelen N, Perfettini I, Zelles T, Aller M, Meyer A, Emptoz A, Giraudet F, Leibovici M, Dartevelle S, Soubigou G, Thiry M, Vizi ES, Safieddine S, Hardelin JP, Avan P, Petit C, Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes., Cell 2015 Nov; 163(4): 894-906.
2015
Urban A, Dussaux C, Martel G, Brunner C, Mace E, Montaldo G, , Real-time imaging of brain activity in freely moving rats using functional ultrasound., Nat Methods 2015 Sep; 12(9): 873-8.
2015
Dahmani M, Ammar-Khodja F, Bonnet C, Lefèvre GM, Hardelin JP, Ibrahim H, Mallek Z, Petit C, EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss, Orphanet J Rare Dis 2015;10:96.
2015
Pepermans E, Petit C, The tip-link molecular complex of the auditory mechano-electrical transduction machinery, Hear. Res. 2015 Dec;330(Pt A):10-7.
2015
Zong L, Guan J, Ealy M, Zhang Q, Wang D, Wang H, Zhao Y, Shen Z, Campbell CA, Wang F, Yang J, Sun W, Lan L, Ding D, Xie L, Qi Y, Lou X, Huang X, Shi Q, Chang S, Xiong W, Yin Z, Yu N, Zhao H, Wang J, Wang J, Salvi RJ, Petit C, Smith RJ, Wang Q, Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder, J. Med. Genet. 2015 May;.
2015
Palacci J, Sacanna S, Abramian A, Barral J, Hanson K, Grosberg AY, Pine DJ, Chaikin PM, Artificial rheotaxis., Sci Adv 2015 May; 1(4): e1400214.
2015
Riahi Z, Bonnet C, Zainine R, Lahbib S, Bouyacoub Y, Bechraoui R, Marrakchi J, Hardelin JP, Louha M, Largueche L, Ben Yahia S, Kheirallah M, Elmatri L, Besbes G, Abdelhak S, Petit C, Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients, PLoS ONE 2015;10(3):e0120584.
2015
Ammar-Khodja F, Bonnet C, Dahmani M, Ouhab S, Lefèvre GM, Ibrahim H, Hardelin JP, Weil D, Louha M, Petit C, Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing, Mol Genet Genomic Med 2015 May;3(3):189-96.
2015
Baldo G, Lorenzini DM, Santos DS, Mayer FQ, Vitry S, Bigou S, Heard JM, Matte U, Giugliani R, , Shotgun proteomics reveals possible mechanisms for cognitive impairment in Mucopolysaccharidosis I mice., Mol. Genet. Metab. 2015 Feb; 114(2): 138-45.
2015
Negre O, Bartholomae C, Beuzard Y, Cavazzana M, Christiansen L, Courne C, Deichmann A, Denaro M, de Dreuzy E, Finer M, Fronza R, Gillet-Legrand B, Joubert C, Kutner R, Leboulch P, Maouche L, Paulard A, Pierciey FJ, Rothe M, Ryu B, Schmidt M, von Kalle C, Payen E, Veres G, , Preclinical evaluation of efficacy and safety of an improved lentiviral vector for the treatment of β-thalassemia and sickle cell disease., Curr Gene Ther 2015 ; 15(1): 64-81.
2014
Merkel M, Sagner A, Gruber FS, Etournay R, Blasse C, Myers E, Eaton S, Jülicher F, The balance of prickle/spiny-legs isoforms controls the amount of coupling between core and fat PCP systems, Curr. Biol. 2014 Sep;24(18):2111-23.
2014
M. Brunstein, R. Braive, R. Hostein, A. Beveratos, I. Robert-Philip, I. Sagnes, T. J. Karle, A. M. Yacomotti, J. A. Levenson, V. Moreau, G. Tessier et Y. De Wilde, Thermo-optical dynamics in an optically pumped Photonic Crystal nano-cavity, Vol 17.
2014
P. Vincent, Y. Bouleau, S. Safieddine, Christine Petit, D. Dulon, Exocytotic Machineries of Vestibular Type I and Cochlear Ribbon Synapses Display Similar Intrinsic Otoferlin-Dependent Ca2+ Sensitivity But a Different Coupling to Ca2+ Channels, Journal of Neuroscience, 2014, 34 (33), pp.10853-10869. ⟨10.1523/JNEUROSCI.0947-14.2014⟩.
2014
Wang H, Zhao Y, Yi Y, Gao Y, Liu Q, Wang D, Li Q, Lan L, Li N, Guan J, Yin Z, Han B, Zhao F, Zong L, Xiong W, Yu L, Song L, Yi X, Yang L, Petit C, Wang Q, Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss, PLoS ONE 2014;9(8):e103133.
2014
Romdhane L, Ben Halim N, Rejeb I, Kefi R, Bouyacoub Y, Ben Rekaya M, Messai H, Messaoud O, Riahi Z, Bonnet C, Ben Rhouma F, Nagara M, Petit C, McElreavey K, Romeo G, Abdelhak S, Specific aspects of consanguinity: some examples from the Tunisian population, Hum. Hered. 2014;77(1-4):167-74.
2014
Michalski N, Petit C, Genetics of auditory mechano-electrical transduction, Pflugers Arch. 2015 Jan;467(1):49-72.
2014
Kazusaku Kamiya, Vincent Michel, Fabrice Giraudet, Brigitte Riederer, Isabelle Foucher, Samantha Papal, Isabelle Perfettini, Sébastien Le Gal, Elisabeth Verpy, Weiliang Xia, Ursula Seidler, Maria-Magdalena Georgescu, Paul Avan, Aziz El-Amraoui, Christine Petit, An unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells, Proceedings of the National Academy of Sciences of the United States of America, 2014, 111 (25), pp.9307-12. ⟨10.1073/pnas.1405322111⟩.
2014
Pepermans E, Michel V, Goodyear R, Bonnet C, Abdi S, Dupont T, Gherbi S, Holder M, Makrelouf M, Hardelin JP, Marlin S, Zenati A, Richardson G, Avan P, Bahloul A, Petit C, The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells, EMBO Mol Med 2014 Jul;6(7):984-92.
2014
Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, Boespflug OT, Besbes G, Abdelhak S, Petit C, Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness, PLoS ONE 2014;9(6):e99797.
2014
Bormuth V, Barral J, Joanny JF, Jülicher F, Martin P, Transduction channels’ gating can control friction on vibrating hair-cell bundles in the ear., Proc Natl Acad Sci U S A 2014 May; 111(20): 7185-90.
2014
Behlouli A, Bonnet C, Abdi S, Bouaita A, Lelli A, Hardelin JP, Schietroma C, Rous Y, Louha M, Cheknane A, Lebdi H, Boudjelida K, Makrelouf M, Zenati A, Petit C, EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness, Orphanet J Rare Dis 2014;9:55.
2014
Brunstein M, Hérault K, Oheim M, , Eliminating unwanted far-field excitation in objective-type TIRF. Part II. combined evanescent-wave excitation and supercritical-angle fluorescence detection improves optical sectioning., Biophys J 2014 Mar; 106(5): 1044-56.
2014
Brunstein M, Teremetz M, Hérault K, Tourain C, Oheim M, , Eliminating unwanted far-field excitation in objective-type TIRF. Part I. identifying sources of nonevanescent excitation light., Biophys J 2014 Mar; 106(5): 1020-32.
2014
Aziz El-Amraoui, Christine Petit, The retinal phenotype of Usher syndrome: Pathophysiological insights from animal models Atteinte rétinienne dans le syndrome de Usher : contribution des modèles animaux à la physiopathologie, Comptes Rendus. Biologies, 2014, 337 (3), pp.167 - 177. ⟨10.1016/j.crvi.2013.12.004⟩.
2014
Elsa Lhériteau, Lolita Petit, Michel Weber, Guylène Le Meur, Jack-Yves Deschamps, Lyse Libeau, Alexandra Mendes-Madeira, Caroline Guihal, Achille François, Richard Guyon, Nathalie Provost, Françoise Lemoine, Samantha Papal, Aziz El-Amraoui, Marie-Anne Colle, Philippe Moullier, Fabienne Rolling, Successful Gene Therapy in the RPGRIP1-deficient Dog: a Large Model of Cone-Rod Dystrophy., Molecular Therapy, 2014, 22 (2), pp.265-77. ⟨10.1038/mt.2013.232⟩.
2013
Bathellier B, Tee SP, Hrovat C, Rumpel S, , A multiplicative reinforcement learning model capturing learning dynamics and interindividual variability in mice., Proc Natl Acad Sci U S A 2013 Dec; 110(49): 19950-5.
2013
Moczulska KE, Tinter-Thiede J, Peter M, Ushakova L, Wernle T, Bathellier B, Rumpel S, , Dynamics of dendritic spines in the mouse auditory cortex during memory formation and memory recall., Proc Natl Acad Sci U S A 2013 Nov; 110(45): 18315-20.
2013
Brunstein M, Wicker K, Hérault K, Heintzmann R, Oheim M, , Full-field dual-color 100-nm super-resolution imaging reveals organization and dynamics of mitochondrial and ER networks., Opt Express 2013 Nov; 21(22): 26162-73.
2013
Meyer A, Petit C, Safieddine S, [Gene therapy for human hearing loss: challenges and promises]., Med Sci (Paris) 2013 Oct; 29(10): 883-9.
2013
Samantha Papal, Matteo Cortese, Kirian Legendre, Nasrin Sorusch, Joseph Dragavon, Iman Sahly, Spencer Shorte, Uwe Wolfrum, Christine Petit, Aziz El-Amraoui, The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route, Human Molecular Genetics, 2013, 22 (18), pp.3773 - 3788. ⟨10.1093/hmg/ddt228⟩.
2013
Lepelletier L, de Monvel JB, Buisson J, Desdouets C, Petit C, Auditory hair cell centrioles undergo confined Brownian motion throughout the developmental migration of the kinocilium, Biophys. J. 2013 Jul;105(1):48-58.
2013
El-Amraoui A, Petit C, , Cadherin defects in inherited human diseases., Prog Mol Biol Transl Sci 2013 ; 116(): 361-84.
2013
Peter M, Bathellier B, Fontinha B, Pliota P, Haubensak W, Rumpel S, , Transgenic mouse models enabling photolabeling of individual neurons in vivo., PLoS One 2013 ; 8(4): e62132.
2012
P. Grinberg, K. Bencheikh, M. Brunstein, A. M. Yacomotti, Y. Dumeige, I. Sagnes, F. Raineri, L. Bigot et J. A. Levenson, Enhancement of a nano cavity lifetime by induced slow light and nonlinear dispersions, Vol 20 .
2012
El-Amraoui A, Petit C, Gene and cell therapies to listen to the inner ear | Les thérapies génique et cellulaire à l’écoute de l’oreille interne, Biofutur, Issue 337, November 2012, Pages 40-42.
2012
El-Amraoui A, Petit C, Hereditary hearing loss | Atteintes héréditaires de l’audition, Biofutur. Issue 337, November 2012, Pages 28-29.
2012
Bathellier B, Ushakova L, Rumpel S, , Discrete neocortical dynamics predict behavioral categorization of sounds., Neuron 2012 Oct; 76(2): 435-49.
2012
Sahly I, Dufour E, Schietroma C, Michel V, Bahloul A, Perfettini I, Pepermans E, Estivalet A, Carette D, Aghaie A, Ebermann I, Lelli A, Iribarne M, Hardelin JP, Weil D, Sahel JA, El-Amraoui A, Petit C, , Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice., J Cell Biol 2012 Oct; 199(2): 381-99.
2012
Charles-Antoine Dutertre, Sonia Amraoui, Annalisa Derosa, Jean-Pierre Jourdain, Lene Vimeux, Matthieu Goguet, Severine Degrelle, Vincent Feuillet, Anne-Sophie Liovat, Michaela Müller-Trutwin, Nipa Decroix, Christiane Deveau, Laurence Meyer, Cécile Goujard, Pierre Loulergue, Odile Launay, Yolande Richard, Anne Hosmalin, Pivotal role of M-DC8+ monocytes from viremic HIV-infected patients in TNF overproduction in response to microbial products., Blood, 2012, 120 (11), pp.2259-2268. ⟨10.1182/blood-2012-03-418681⟩.
2012
P. Grinberg, K. Bencheikh, M. Brunstein, A. M. Yacomotti, Y. Dumeige, I. Sagnes, F. Raineri, L. Bigot et J. A. Levenson, Nanocavity Linewidth Narrowing and Group Delay Enhancement by Slow Light Propagation and Nonlinear Effects, Vol 109.
2012
Delmaghani S, Aghaie A, Michalski N, Bonnet C, Weil D, Petit C, Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness, Hum. Mol. Genet. 2012 Sep;21(17):3835-44.
2012
Barral J, Martin P, Phantom tones and suppressive masking by active nonlinear oscillation of the hair-cell bundle., Proc Natl Acad Sci U S A 2012 May; 109(21): E1344-51.
2012
M. Brunstein, A. M. Yacomotti, I. Sagnes, F. Raineri, L. Bigot, et A. Levenson, Excitability and self pulsing in a Photonic Crystal Nanocavity, Vol. 85.
2012
Bonnet C, El-Amraoui A, , Usher syndrome (sensorineural deafness and retinitis pigmentosa): pathogenesis, molecular diagnosis and therapeutic approaches., Curr Opin Neurol 2012 Feb; 25(1): 42-9.
2012
Safieddine S, El-Amraoui A, Petit C, The auditory hair cell ribbon synapse: from assembly to function., Annu Rev Neurosci 2012 ; 35(): 509-28.
2011
Barral J, Martin P, The physical basis of active mechanosensitivity by the hair-cell bundle., Curr Opin Otolaryngol Head Neck Surg 2011 Oct; 19(5): 369-75.
2011
M. Brunstein, T. J. Karle, I. Sagnes, F. Raineri, J. Bloch, Y. Halioua, G. Beaudoin, L. Le Gratiet, J. A. Levenson, et A. M. Yacomotti, Radiation patterns from coupled photonic crystal nanocavities, Vol 99.
2011
Ronen K, Negre O, Roth S, Colomb C, Malani N, Denaro M, Brady T, Fusil F, Gillet-Legrand B, Hehir K, Beuzard Y, Leboulch P, Down JD, Payen E, Bushman FD, , Distribution of lentiviral vector integration sites in mice following therapeutic gene transfer to treat β-thalassemia., Mol Ther 2011 Jul; 19(7): 1273-86.
2011
Negre O, Fusil F, Colomb C, Roth S, Gillet-Legrand B, Henri A, Beuzard Y, Bushman F, Leboulch P, Payen E, , Correction of murine β-thalassemia after minimal lentiviral gene transfer and homeostatic in vivo erythroid expansion., Blood 2011 May; 117(20): 5321-31.
2011
Crystel Bonnet, M'Hamed Grati, Sandrine Marlin, Jacqueline Levilliers, Jean-Pierre Hardelin, Marine Parodi, Magali Niasme-Grare, Diana Zelenika, Marc Délépine, Delphine Feldmann, Laurence Jonard, Aziz El-Amraoui, Dominique Weil, Bruno Delobel, Christophe Vincent, Hélène Dollfus, Marie-Madeleine Eliot, Albert David, Catherine Calais, Jacqueline Vigneron, Bettina Montaut-Verient, Dominique Bonneau, Jacques Dubin, Christel Thauvin, Alain Duvillard, Christine Francannet, Thierry Mom, Didier Lacombe, Françoise Duriez, Valérie Drouin-Garraud, Marie-Françoise Thuillier-Obstoy, Sabine Sigaudy, Anne-Marie Frances, Patrick Collignon, Georges Challe, Rémy Couderc, Mark Lathrop, José-Alain Sahel, Jean Weissenbach, Christine Petit, Françoise Denoyelle, Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis., Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.21. ⟨10.1186/1750-1172-6-21⟩.
2011
Caberlotto E, Michel V, Foucher I, Bahloul A, Goodyear RJ, Pepermans E, Michalski N, Perfettini I, Alegria-Prévot O, Chardenoux S, Do Cruzeiro M, Hardelin JP, Richardson GP, Avan P, Weil D, Petit C, Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia, Proc. Natl. Acad. Sci. U.S.A. 2011 Apr;108(14):5825-30.
2011
Aigouy B, Etournay R, Sagner A, Staple DB, Farhadifar R, Röper JC, Eaton S, Jülicher F, [Cell flow reorients planar polarity in the wing of Drosophila], Med Sci (Paris) 2011 Feb;27(2):117-9.
2011
Verpy E, Leibovici M, Michalski N, Goodyear RJ, Houdon C, Weil D, Richardson GP, Petit C, Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane, J. Comp. Neurol. 2011 Feb;519(2):194-210.
2010
Heard JM, Bruyère J, Roy E, Bigou S, Ausseil J, Vitry S, , Storage problems in lysosomal diseases., Biochem. Soc. Trans. 2010 Dec; 38(6): 1442-7.
2010
El-Amraoui A, Petit C, , [Stem cell therapy in the inner ear: recent achievements and prospects]., Med Sci (Paris) 2010 Nov; 26(11): 981-5.
2010
Beurg M, Michalski N, Safieddine S, Bouleau Y, Schneggenburger R, Chapman ER, Petit C, Dulon D, Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells., J Neurosci 2010 Oct; 30(40): 13281-90.
2010
Cavazzana-Calvo M, Payen E, Negre O, Wang G, Hehir K, Fusil F, Down J, Denaro M, Brady T, Westerman K, Cavallesco R, Gillet-Legrand B, Caccavelli L, Sgarra R, Maouche-Chrétien L, Bernaudin F, Girot R, Dorazio R, Mulder GJ, Polack A, Bank A, Soulier J, Larghero J, Kabbara N, Dalle B, Gourmel B, Socie G, Chrétien S, Cartier N, Aubourg P, Fischer A, Cornetta K, Galacteros F, Beuzard Y, Gluckman E, Bushman F, Hacein-Bey-Abina S, Leboulch P, , Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia., Nature 2010 Sep; 467(7313): 318-22.
2010
M. Brunstein, A. Yacomotti, R. Braive, S. Barbay, I. Sagnes, L. Bigot, L. Le-Gratiet et J. A. Levenson, All-optical, all-fibered ultrafast switching in 2D InP-based photonic crystal nanocavity, Vol 4.
2010
Bahloul A, Michel V, Hardelin JP, Nouaille S, Hoos S, Houdusse A, England P, Petit C, Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids, Hum. Mol. Genet. 2010 Sep;19(18):3557-65.
2010
Boutet de Monvel J, Petit C, Wrapping up stereocilia rootlets, Cell 2010 May;141(5):748-50.
2010
Barral J, Dierkes K, Lindner B, Jülicher F, Martin P, Coupling a sensory hair-cell bundle to cyber clones enhances nonlinear amplification., Proc Natl Acad Sci U S A 2010 May; 107(18): 8079-84.
2010
Etournay R, Lepelletier L, Boutet de Monvel J, Michel V, Cayet N, Leibovici M, Weil D, Foucher I, Hardelin JP, Petit C, Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape, Development 2010 Apr;137(8):1373-83.
2010
V. Moreau, G. Tessier, Y. De Wilde, M. Brunstein, A. Yacomotti, F. Raineri, R. Raj, I. Sagnes, R. Braive et A. Levenson, Transient ThermoReflectance Imaging of Active Photonic Crystals, Vol 96.
2010
L. C. Estrada, O. E. Martinez, M. Brunstein, S. Bouchoule, L. Le-Gratiet, A. Talneau, I. Sagnes, P. Monnier, J. A. Levenson et A. M. Yacomotti , Small volume excitation and enhancement of dye fluorescence on a 2D photonic crystal surface, Vol 18.
2010
El-Amraoui A, Petit C, , Cadherins as targets for genetic diseases., Cold Spring Harb Perspect Biol 2010 Jan; 2(1): a003095.
2010
Hocquemiller M, Vitry S, Bigou S, Bruyère J, Ausseil J, Heard JM, , GAP43 overexpression and enhanced neurite outgrowth in mucopolysaccharidosis type IIIB cortical neuron cultures., J. Neurosci. Res. 2010 Jan; 88(1): 202-13.
2009
Roux I, Hosie S, Johnson SL, Bahloul A, Cayet N, Nouaille S, Kros CJ, Petit C, Safieddine S, Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses., Hum Mol Genet 2009 Dec; 18(23): 4615-28.
2009
Michalski N, Michel V, Caberlotto E, Lefèvre GM, van Aken AF, Tinevez JY, Bizard E, Houbron C, Weil D, Hardelin JP, Richardson GP, Kros CJ, Martin P, Petit C, , Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells., Pflugers Arch 2009 Nov; 459(1): 115-30.
2009
del Castillo FJ, Cohen-Salmon M, Charollais A, Caille D, Lampe PD, Chavrier P, Meda P, Petit C, Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins, Hum. Mol. Genet. 2010 Jan;19(2):262-75.
2009
Brunstein M, Bruno L, Desposito M, Levi V, , Anomalous dynamics of melanosomes driven by myosin-V in Xenopus laevis melanophores., Biophys J 2009 Sep; 97(6): 1548-57.
2009
Dulon D, Safieddine S, Jones SM, Petit C, Otoferlin is critical for a highly sensitive and linear calcium-dependent exocytosis at vestibular hair cell ribbon synapses., J Neurosci 2009 Aug; 29(34): 10474-87.
2009
L. Bruno, V. Levi, M. Brunstein, et M. A. Desposito, Transition to superdiffusive behavior in intracellular actin-based transport mediated by molecular motors, Vol 80.
2009
Kirian Legendre, Christine Petit et Aziz El-Amraoui*, The outer hair cell of the mammalian cochlea: An outstanding amplifier | La cellule ciliée externe de la cochlée des mammifères: Un amplificateur aux propriétés exceptionnelles, Med Sci (Paris) 2009 ; 25 : 117–120.
2009
Petit C, Richardson GP, Linking genes underlying deafness to hair-bundle development and function, Nat. Neurosci. 2009 Jun;12(6):703-10.
2009
Bahloul A, Simmler MC, Michel V, Leibovici M, Perfettini I, Roux I, Weil D, Nouaille S, Zuo J, Zadro C, Licastro D, Gasparini P, Avan P, Hardelin JP, Petit C, Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells, EMBO Mol Med 2009 May;1(2):125-38.
2009
Legendre K, Petit C, El-Amraoui A, , [The outer hair cell of the mammalian cochlea: an outstanding amplifier]., Med Sci (Paris) 2009 Feb; 25(2): 117-20.
2008
Aziz El-Amraoui, Amel Bahloul, Christine Petit, Myosin VII, Myosins pp 353-373.
2008
Kirian Legendre, Saaid Safieddine, Polonca Küssel-Andermann, Christine Petit, Aziz El-Amraoui, αII-βV spectrin bridges the plasma membrane and cortical lattice in the lateral wall of the auditory outer hair cells, Journal of Cell Science, 2008, 121 (20), pp.3347-3356. ⟨10.1242/jcs.028134⟩.
2008
Verpy E, Weil D, Leibovici M, Goodyear RJ, Hamard G, Houdon C, Lefèvre GM, Hardelin JP, Richardson GP, Avan P, Petit C, Stereocilin-deficient mice reveal the origin of cochlear waveform distortions, Nature 2008 Nov;456(7219):255-8.
2008
Lefèvre G, Michel V, Weil D, Lepelletier L, Bizard E, Wolfrum U, Hardelin JP, Petit C, A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth, Development 2008 Apr;135(8):1427-37.
2008
Beurg M, Safieddine S, Roux I, Bouleau Y, Petit C, Dulon D, Calcium- and otoferlin-dependent exocytosis by immature outer hair cells., J Neurosci 2008 Feb; 28(8): 1798-803.
2008
Michel Leibovici, Saaid Safieddine, Christine Petit, [Chapter 8] Mouse Models for Human Hereditary Deafness, Mouse Models of Developmental Genetic Disease, 84, Elsevier, pp.385-429, 2008, Current Topics in Developmental Biology, 978-0-12-374454-8. ⟨10.1016/S0070-2153(08)00608-X⟩.
2007
Raphael Etournay, Ingrid Zwaenepoel, Isabelle Perfettini, Pierre Legrain, Christine Petit, Aziz El-Amraoui, Shroom2, a myosin-VIIa- and actin-binding protein, directly interacts with ZO-1 at tight junctions., Journal of Cell Science, 2007, 120 (16), pp.2838-50. ⟨10.1242/jcs.002568⟩.
2007
Michalski N, Michel V, Bahloul A, Lefèvre G, Barral J, Yagi H, Chardenoux S, Weil D, Martin P, Hardelin JP, Sato M, Petit C, Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning., J Neurosci 2007 Jun; 27(24): 6478-88.
2006
Roux I, Safieddine S, Nouvian R, Grati M, Simmler MC, Bahloul A, Perfettini I, Le Gall M, Rostaing P, Hamard G, Triller A, Avan P, Moser T, Petit C, Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse., Cell 2006 Oct; 127(2): 277-89.
2006
Isabelle Roux, Saaid Safieddine, Régis Nouvian, M'Hamed Grati, Marie-Christine Simmler, Amel Bahloul, Isabelle Perfettini, Morgane Le Gall, Phillipe Rostaing, Ghislaine Hamard, Antoine Triller, Paul Avan, Tobias Moser, Christine Petit, Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse., Cell, 2006, 127 (2), pp.277-89. ⟨10.1016/j.cell.2006.08.040⟩.
2006
Delmaghani S, del Castillo FJ, Michel V, Leibovici M, Aghaie A, Ron U, Van Laer L, Ben-Tal N, Van Camp G, Weil D, Langa F, Lathrop M, Avan P, Petit C, Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy, Nat. Genet. 2006 Jul;38(7):770-8.
2006
Petit C, From deafness genes to hearing mechanisms: harmony and counterpoint, Trends Mol Med 2006 Feb;12(2):57-64.
2005
Avital Adato, Gaëlle Lefèvre, Benjamin Delprat, Vincent Michel, Nicolas Michalski, Sébastien Chardenoux, Dominique Weil, Aziz El-Amraoui, Christine Petit, Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells, Human Molecular Genetics, 2005, 14 (24), pp.3921 - 3932. ⟨10.1093/hmg/ddi416⟩.
2005
Hyenne V, Louvet-Vallée S, El-Amraoui A, Petit C, Maro B, Simmler MC, , Vezatin, a protein associated to adherens junctions, is required for mouse blastocyst morphogenesis., Dev Biol 2005 Nov; 287(1): 180-91.
2005
Aziz El-Amraoui, Christine Petit, Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells, Journal of Cell Science, 2005, 118 (20), pp.4593-4603. ⟨10.1242/jcs.02636⟩.
2005
Aziz El-Amraoui, Gaëlle Lefèvre, Jean-Pierre Hardelin, Christine Petit, Syndrome de Usher de type 1 et développement de la touffe ciliaire des cellules sensorielles de l’oreille interne Usher syndrome type I and the differentiation of inner ear sensory cells’ hair bundles, médecine/sciences, 2005, 21 (8-9), pp.737-40. ⟨10.1051/medsci/2005218-9737⟩.
2005
Raphael Etournay, Aziz El-Amraoui, Amel Bahloul, Stéphane Blanchard, Isabelle Roux, Guillaume Pézeron, Nicolas Michalski, Laurent Daviet, Jean-Pierre Hardelin, Pierre Legrain, Christine Petit, PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa., Journal of Cell Science, 2005, 118 (13), pp.2891-99. ⟨10.1242/jcs.02424⟩.
2005
Leibovici M, Verpy E, Goodyear RJ, Zwaenepoel I, Blanchard S, Lainé S, Richardson GP, Petit C, Initial characterization of kinocilin, a protein of the hair cell kinocilium, Hear. Res. 2005 May;203(1-2):144-53.
2005
Michel V, Goodyear RJ, Weil D, Marcotti W, Perfettini I, Wolfrum U, Kros CJ, Richardson GP, Petit C, Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells, Dev. Biol. 2005 Apr;280(2):281-94.
2005
Avital Adato, Vincent Michel, Yoshiaki Kikkawa, Jan Reiners, Kumar N Alagramam, Dominique Weil, Hiromichi Yonekawa, Uwe Wolfrum, Aziz El-Amraoui, Christine Petit, Interactions in the network of Usher syndrome type 1 proteins, Human Molecular Genetics, 2004, 14, pp.347 - 356. ⟨10.1093/hmg/ddi031⟩.
2005
Benjamin Delprat, Vincent Michel, Richard Goodyear, Yasuhiro Yamasaki, Nicolas Michalski, Aziz El-Amraoui, Isabelle Perfettini, Pierre Legrain, Guy Richardson, Jean-Pierre Hardelin, Christine Petit, Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly, Human Molecular Genetics, 2004, 14 (3), pp.401 - 410. ⟨10.1093/hmg/ddi036⟩.
2004
Petit C, Memorial lecture-hereditary sensory defects: from genes to pathogenesis, Am. J. Med. Genet. A 2004 Sep;130A(1):3-7.
2004
Sandra Sousa, Didier Cabanes, Aziz El-Amraoui, Christine Petit, Marc Lecuit, Pascale Cossart, Unconventional myosin VIIa and vezatin, two proteins crucial for Listeria entry into epithelial cells, Journal of Cell Science, 2004, 117 (Pt 10), pp.2121-2130. ⟨10.1242/jcs.01066⟩.
2004
Hardelin JP, Denoyelle F, Levilliers J, Simmler MC, Petit C, [Hereditary deafness: molecular genetics], Med Sci (Paris) 2004 Mar;20(3):311-6.
2004
Cohen-Salmon M, Maxeiner S, Krüger O, Theis M, Willecke K, Petit C, Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear, Cell Tissue Res. 2004 Apr;316(1):15-22.
2003
Claire Desnos, Jean-Sébastien Schonn, Sébastien Huet, Viet Samuel Tran, Aziz El-Amraoui, Graça Raposo, Isabelle Fanget, Catherine Chapuis, Gaël Ménasché, Geneviève de Saint Basile, Christine Petit, Sophie Cribier, Jean-Pierre Henry, François Darchen, Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites, Journal of Cell Biology, 2003, 163 (3), pp.559. ⟨10.1083/jcb.200302157⟩.
2003
Reiners J, Reidel B, El-Amraoui A, Boëda B, Huber I, Petit C, Wolfrum U, , Differential distribution of harmonin isoforms and their possible role in Usher-1 protein complexes in mammalian photoreceptor cells., Invest Ophthalmol Vis Sci 2003 Nov; 44(11): 5006-15.
2003
Delmaghani S, Aghaie A, Compain-Nouaille S, Ataie A, Lemainque A, Zeinali S, Lathrop M, Weil D, Petit C, DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1, Eur. J. Hum. Genet. 2003 Oct;11(10):816-8.
2003
Waselle L, Coppola T, Fukuda M, Iezzi M, El-Amraoui A, Petit C, Regazzi R, , Involvement of the Rab27 binding protein Slac2c/MyRIP in insulin exocytosis., Mol Biol Cell 2003 Oct; 14(10): 4103-13.
2003
Philomena Mburu, Mirna Mustapha, Anabel Varela, Dominique Weil, Aziz El-Amraoui, Ralph H Holme, Andreas Rump, Rachel E Hardisty, Stéphane Blanchard, Roney S Coimbra, Isabelle Perfettini, Nick Parkinson, Ann-Marie Mallon, Pete Glenister, Mike J Rogers, Adam J Paige, Lee Moir, Jo Clay, Andre Rosenthal, Xue Zhong Liu, Gonzalo Blanco, Karen P Steel, Christine Petit, Steve D M Brown, Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31, Nature Genetics, 2003, 34, pp.421-428. ⟨10.1038/ng1208⟩.
2003
Weil D, El-Amraoui A, Masmoudi S, Mustapha M, Kikkawa Y, Lainé S, Delmaghani S, Adato A, Nadifi S, Zina ZB, Hamel C, Gal A, Ayadi H, Yonekawa H, Petit C, , Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin., Hum Mol Genet 2003 Mar; 12(5): 463-71.
2002
Boëda B, El-Amraoui A, Bahloul A, Goodyear R, Daviet L, Blanchard S, Perfettini I, Fath KR, Shorte S, Reiners J, Houdusse A, Legrain P, Wolfrum U, Richardson G, Petit C, , Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle., EMBO J 2002 Dec; 21(24): 6689-99.
2002
Cohen-Salmon M, Ott T, Michel V, Hardelin JP, Perfettini I, Eybalin M, Wu T, Marcus DC, Wangemann P, Willecke K, Petit C, Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death, Curr. Biol. 2002 Jul;12(13):1106-11.
2002
Coimbra RS, Weil D, Brottier P, Blanchard S, Levi M, Hardelin JP, Weissenbach J, Petit C, A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear, Genome Res. 2002 Jun;12(6):1007-11.
2002
Lee HK, Safieddine S, Petralia RS, Wenthold RJ, Identification of a novel SNAP25 interacting protein (SIP30)., J Neurochem 2002 Jun; 81(6): 1338-47.
2002
Eybalin M, Renard N, Aure F, Safieddine S, Cysteine-string protein in inner hair cells of the organ of Corti: synaptic expression and upregulation at the onset of hearing., Eur J Neurosci 2002 May; 15(9): 1409-20.
2002
Soussi-Yanicostas N, de Castro F, Julliard AK, Perfettini I, Chédotal A, Petit C, Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons, Cell 2002 Apr;109(2):217-28.
2002
El-Amraoui A, Schonn JS, Küssel-Andermann P, Blanchard S, Desnos C, Henry JP, Wolfrum U, Darchen F, Petit C, , MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes., EMBO Rep 2002 May; 3(5): 463-70.
2002
Mustapha M, Chouery E, Torchard-Pagnez D, Nouaille S, Khrais A, Sayegh FN, Mégarbané A, Loiselet J, Lathrop M, Petit C, Weil D, A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25, Hum. Genet. 2002 Apr;110(4):348-50.
2002
Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C, DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34, Eur. J. Hum. Genet. 2002 Mar;10(3):210-2.
2002
Denoyelle F, Mustapha M, Petit C, DFNB21, Adv. Otorhinolaryngol. 2002;61:153-5.
2002
Denoyelle F, Petit C, DFNB9, Adv. Otorhinolaryngol. 2002;61:142-4.
2002
Wenthold RJ, Safieddine S, Ly CD, Wang YX, Lee HK, Wang CY, Kachar B, Petralia RS, Vesicle targeting in hair cells., Audiol Neurootol 2002 ; 7(1): 45-8.
2001
El-Amraoui A, Cohen-Salmon M, Petit C, Simmler MC, Spatiotemporal expression of otogelin in the developing and adult mouse inner ear, Hear. Res. 2001 Aug;158(1-2):151-9.
2000
Polonca Küssel-Andermann, Aziz El-Amraoui, Saaid Safieddine, Sylvie Nouaille, Isabelle Perfettini, Marc Lecuit, Pascale Cossart, Uwe Wolfrum, Christine Petit, Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex, EMBO Journal, 2000, 19 (22), pp.6020-6029. ⟨10.1093/emboj/19.22.6020⟩.
2000
Polonca Küssel-Andermann, Aziz El-Amraoui, Saaid Safieddine, Jean-Pierre Hardelin, Sylvie Nouaille, Jacques Camonis, Christine Petit, Unconventional Myosin VIIA Is a Novel A-kinase-anchoring Protein, Journal of Biological Chemistry, 2000, 275 (38), pp.29654-29659. ⟨10.1074/jbc.M004393200⟩.
2000
Kharkovets T, Hardelin JP, Safieddine S, Schweizer M, El-Amraoui A, Petit C, Jentsch TJ, KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway., Proc Natl Acad Sci U S A 2000 Apr; 97(8): 4333-8.
2000
Simmler MC, Cohen-Salmon M, El-Amraoui A, Guillaud L, Benichou JC, Petit C, Panthier JJ, Targeted disruption of otog results in deafness and severe imbalance, Nat. Genet. 2000 Feb;24(2):139-43.
1999
Shin'Ichiro Yasunaga, M'Hamed Grati, Martine Cohen-Salmon, Aziz El-Amraoui, Mirna Mustapha, Nabiha Salem, Elie El-Zir, Jacques Loiselet, Christine Petit, A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness, Nature Genetics, 1999, 21 (4), pp.363-369. ⟨10.1038/7693⟩.
1999
Christian Kubisch, Björn Schroeder, Thomas Friedrich, Björn Lütjohann, Aziz El-Amraoui, Sandrine Marlin, Christine Petit, Thomas Jentsch, KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness, Cell, 1999, 96 (3), pp.437-446. ⟨10.1016/s0092-8674(00)80556-5⟩.
1998
Vasiliki Kalatzis, Iman Sahly, Aziz El-Amraoui, Christine Petit, Eya1 expression in the developing ear and kidney: Towards the understanding of the pathogenesis of branchio-oto-renal (BOR) syndrome, Developmental Dynamics, 1998, 213 (4), pp.486-499. <a target="_blank" href="https://dx.doi.org/10.1002/(SICI)1097-0177(199812)213:43.0.CO;2-L">⟨10.1002/(SICI)1097-0177(199812)213:43.0.CO;2-L⟩.
1997
Cohen-Salmon M, El-Amraoui A, Leibovici M, Petit C, Otogelin: a glycoprotein specific to the acellular membranes of the inner ear, Proc. Natl. Acad. Sci. U.S.A. 1997 Dec;94(26):14450-5.
1997
El-Amraoui A, Petit C, Towards a molecular understanding of the pathophysiology of Usher syndrome, Journal of Audiological MedicineVolume 6, Issue 3, 1997, Pages 170-184.
1997
Paul Dubois, Aziz El Amraoui, Anne Héritier, Development and differentiation of pituitary cells, Microscopy Research and Technique, 1997, Special Issue: Functional Anatomy of the Pituitary Gland and Alterations in Disease, 39 (2), pp.98-113. <a target="_blank" href="https://dx.doi.org/10.1002/(SICI)1097-0029(19971015)39:23.0.CO;2-S">⟨10.1002/(SICI)1097-0029(19971015)39:23.0.CO;2-S⟩.
1997
Iman Sahly, Aziz El-Amraoui, Marc Abitbol, Christine Petit, Jean-Louis Dufier, Expression of myosin VIIA during mouse embryogenesis, Anatomy and Embryology, 1997, 196 (2), pp.159-170. ⟨10.1007/s004290050088⟩.
1997
Fabien Crozet, Aziz El Amraoui, Stéphane Blanchard, Marc Lenoir, Chantal Ripoll, Philippe Vago, Christian Hamel, Cécile Fizames, Fabienne Levi-Acobas, Danièle Depétris, Marie-Genevı̀eve Mattei, Dominique Weil, Rémy Pujol, Christine Petit, Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins, Genomics, 1997, 40 (2), pp.332-341. ⟨10.1006/geno.1996.4526⟩.
1996
Catherine Verney, Aziz El Amraoui, Nada Zecevic, Comigration of tyrosine hydroxylase- and gonadotropin-releasing hormone-immunoreactive neurons in the nasal area of human embryos, Developmental Brain Research, 1996, 97 (2), pp.251-259. ⟨10.1016/s0165-3806(96)00147-2⟩.
1996
A El-Amraoui, Iman Sahly, Serge Picaud, José Sahel, Marc Abitbol, Christine Petit, Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells, Human Molecular Genetics, 1996, 5 (8), pp.1171-1178. ⟨10.1093/hmg/5.8.1171⟩.
1996
D Weil, G Levy, I Sahly, F Levi-Acobas, S Blanchard, A El-Amraoui, F Crozet, H Philippe, M Abitbol, C Petit, Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia., Proceedings of the National Academy of Sciences of the United States of America, 1996, 93 (8), pp.3232-3237. ⟨10.1073/pnas.93.8.3232⟩.
1995
Elamraoui A, Berghman LR, Dubois PM, Interactions between adenohypophyseal, hypothalamic and nasal presumptive territories during early neurulation process, Endocrine 1995 May;3(5):335-43.
1993
Aziz Elamraoui, Paul Dubois, Experimental Evidence for the Early Commitment of the Presumptive Adenohypophysis, Neuroendocrinology, 2004, 58 (6), pp.609-615. ⟨10.1159/000126599⟩.
1993
el Amraoui A, Dubois PM, Experimental evidence for an early commitment of gonadotropin-releasing hormone neurons, with special regard to their origin from the ectoderm of nasal cavity presumptive territory, Neuroendocrinology 1993 Jun;57(6):991-1002.
1992
Safieddine S, Eybalin M, Triple Immunofluorescence Evidence for the Coexistence of Acetylcholine, Enkephalins and Calcitonin Gene-related Peptide Within Efferent (Olivocochlear) Neurons of Rats and Guinea-pigs., Eur J Neurosci 1992 ; 4(10): 981-992.